irAE Prediction of Anti-PD-1/L1 in Lung Cancer

Status Recruiting

Clinical Trial Summary

the purpose of this study is to identify multi-dimensional immunological biomarkers including cytokines, autoantibodies, and immune cell subtypes of immune-related adverse events (primary) and prognosis(secondary) in the anti-PD-1/anti-PD-L1 immunotherapy for lung cancer

Clinical Trial Description

After being informed of the study and potential risk, all patients giving written informed consent will undergo peripheral blood sample collection at baseline (before treatment ), 1month and 3month after treatment initiation, and when immune-related adverse events ever occur. The follow-up period will be 1 year for any occurrence of immune-related adverse events and 2 years follow-up for the prognosis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05288569
Study type	Observational
Source	Peking Union Medical College Hospital
Contact	Huaxia Yang
Phone	+86-13488869596
Email	yanghuaxia2013@163.com
Status	Recruiting
Phase
Start date	January 21, 2022
Completion date	September 2024

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